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review of literature on clinical pancreatology - The Pancreapedia

review of literature on clinical pancreatology - The Pancreapedia

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Chr<strong>on</strong>ic pancreatitis is associated with a substantial morbidity, including malnutriti<strong>on</strong>,malabsorpti<strong>on</strong>, pseudocysts, metabolic disturbances, and intractable abdominal pain.Approximately 5 percent <str<strong>on</strong>g>of</str<strong>on</strong>g> patients with chr<strong>on</strong>ic pancreatitis are refractory to nutriti<strong>on</strong>alsupport and opiate analgesia, making management challenging. Pancreatic rest can providesymptomatic relief. However, achieving simultaneous pancreatic rest and adequatenutriti<strong>on</strong>al support in these patients is difficult. It was describe a technique for providingnutriti<strong>on</strong>al support and pancreatic rest in patients with intractable symptomatic in 3 patients.All 3 patients had masses associated with the pancreas. Symptom relief and adequatenutriti<strong>on</strong>al support were achieved by inserting a l<strong>on</strong>g-term nasojejunal tube (FlocareBengmark, Nutricia Clinical Care, United Kingdom) under ambulatory endoscopic guidance.<strong>The</strong> l<strong>on</strong>g-term nasojejunal tube feeding achieved pancreatic rest and significant symptomaticrelief while delivering adequate nutriti<strong>on</strong>al support. Pseudocyst size decreased substantiallyin 2 patients. <strong>The</strong> third patient was found to have pancreatic carcinoma afterpancreaticoduodenectomy [288].Influence <str<strong>on</strong>g>of</str<strong>on</strong>g> colostrumsExocrine pancreatic secreti<strong>on</strong> c<strong>on</strong>tributes to limit pathogenic bacteria-associated diarrhea.Bovine colostrum, used in the treatment <str<strong>on</strong>g>of</str<strong>on</strong>g> diarrhea, reduces symptoms originating from gutpathogenic bacteria overgrowth. It was hypothesized that bovine colostrum may stimulate theexocrine pancreatic secreti<strong>on</strong>. Eighteen piglets fitted with 2 permanent catheters (forpancreatic juice collecti<strong>on</strong> and reintroducti<strong>on</strong>) were allocated to 1 <str<strong>on</strong>g>of</str<strong>on</strong>g> the following 2 dietarytreatments for 5 days: a c<strong>on</strong>trol diet or a diet supplemented with defatted bovine colostrum.Pancreatic juice was collected daily, and digestive enzyme activities and antibacterial activitywere determined. <strong>The</strong> prandial pancreatic juice outflow, the basal and prandial lipase output,and the basal secreti<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> the antibacterial activity were, respectively, 60 percent, 154percent, 92 percent, and 72 percent higher in piglets fed a diet supplemented with defattedbovine colostrum. It was c<strong>on</strong>cluded that with defatted bovine colostrum, the increasedantibacterial activity secreti<strong>on</strong> against Escherichia coli may limit pathogenic bacteriaovergrowth <str<strong>on</strong>g>of</str<strong>on</strong>g> the gut and reduce diarrheal episodes. <strong>The</strong> role <str<strong>on</strong>g>of</str<strong>on</strong>g> secretin in the increasedpancreatic juice flow and lipase secreti<strong>on</strong> was c<strong>on</strong>sidered [289].Diabetes in chr<strong>on</strong>ic pancreatitisIn c<strong>on</strong>sequence <str<strong>on</strong>g>of</str<strong>on</strong>g> the close anatomical and functi<strong>on</strong>al links between the exocrine andendocrine pancreas, any disease affecting <strong>on</strong>e <str<strong>on</strong>g>of</str<strong>on</strong>g> these parts will inevitably affect the other.Pancreatic c<strong>on</strong>diti<strong>on</strong>s which might cause diabetes mellitus include acute and chr<strong>on</strong>icpancreatitis, pancreatic surgery, cystic fibrosis and pancreatic cancer. <strong>The</strong> development <str<strong>on</strong>g>of</str<strong>on</strong>g>diabetes greatly influences the prognosis and quality <str<strong>on</strong>g>of</str<strong>on</strong>g> life <str<strong>on</strong>g>of</str<strong>on</strong>g> patients with exocrinepancreatic diseases. It may cause lifethreatening complicati<strong>on</strong>s, such as hypoglycemia, dueto the lack <str<strong>on</strong>g>of</str<strong>on</strong>g> glucag<strong>on</strong> and the impaired absorpti<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> nutrients, or the micro- andmacrovascular complicati<strong>on</strong>s may impair the organ functi<strong>on</strong>s. Temporary hyperglycemia canbe observed in around 50 percent <str<strong>on</strong>g>of</str<strong>on</strong>g> patients with acute pancreatitis; persisting diabetesmellitus may affect 1-15 percent. <strong>The</strong> prevalence <str<strong>on</strong>g>of</str<strong>on</strong>g> diabetes in chr<strong>on</strong>ic pancreatitis variesbetween 30 and 83 percent. Overall, exocrine pancreatic diseases are believed to beresp<strong>on</strong>sible for diabetes in <strong>on</strong>ly about 0.5-1.7 percent <str<strong>on</strong>g>of</str<strong>on</strong>g> the cases, but in as many as 15-20percent <str<strong>on</strong>g>of</str<strong>on</strong>g> diabetes mellitus patients in Southeast Asia, where tropical pancreatitis isendemic. <strong>The</strong> incidence <str<strong>on</strong>g>of</str<strong>on</strong>g> pancreatic diabetes depends <strong>on</strong> several factors, such as theetiology and durati<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> chr<strong>on</strong>ic pancreatitis, and the presence <str<strong>on</strong>g>of</str<strong>on</strong>g> pancreatic calcificati<strong>on</strong>.<strong>The</strong> endocrine functi<strong>on</strong> is more disturbed in alcoholic chr<strong>on</strong>ic pancreatitis than inn<strong>on</strong>alcoholic pancreatitis. Both insulin and glucag<strong>on</strong> secreti<strong>on</strong> are more str<strong>on</strong>gly impaired inpatients with calcified chr<strong>on</strong>ic pancreatitis than in those with n<strong>on</strong>calcified chr<strong>on</strong>ic pancreatitis.In two recent follow-up studies <str<strong>on</strong>g>of</str<strong>on</strong>g> patients with chr<strong>on</strong>ic pancreatitis over a period <str<strong>on</strong>g>of</str<strong>on</strong>g> 7.7 and 8

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